FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term X-linked spondyloepiphyseal dysplasia tarda ID (Ontology) DOID:0080362 (Human Disease)
Definition A spondyloepiphyseal dysplasia that is characterized by impaired growth of bones of the spine and the ends of long bones in the arms and legs and has_material_basis_in mutation in the SEDL gene on chromosome Xp22.
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 Genes
 X-linked spondyloepiphyseal dysplasia tarda       1
 for disease ribbon | X-linked spondyloepiphyseal dysplasia tarda       1
 model of | X-linked spondyloepiphyseal dysplasia tarda       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease__________
bone disease                            |
 |__spinal disease______________________|
spondyloepiphyseal dysplasia            |
 |__spondyloepiphyseal dysplasia tarda__|
                                        X-linked spondyloepiphyseal dysplasia tarda  1 rec.
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Is a spinal disease
X-linked recessive disease
spondyloepiphyseal dysplasia tarda
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MIM:313400